Lieberman notes that her laboratory reported a similar reaction to perforin, granulysin and
granzyme in intracellular bacteria in a 2014 Cell paper.
Not exact matches
Particularly prominent
in the RNA - Seq analysis was the up - regulation of a number of
granzymes, a group of proteinases secreted by immune cells that were originally thought to be involved
in killing (via apoptosis) virus infected cells or other target cells.
They also found elevated
granzyme A levels
in blood samples taken from non-human primates infected with chikungunya, as well as from human chikungunya patients.
NK cells are cytotoxic; small granules
in their cytoplasm contain special proteins such as perforin and proteases known as
granzymes.
Perforin pores
in the endosomal membrane trigger the release of endocytosed
granzyme B into the cytosol of target cells.
Consistent with previously reported analyses, we also observed enhanced IFN - γ and
granzyme B production
in DGKζ and Cbl - b — deficient T cells.
Further, although we could detect enhancement of
granzyme B production
in DKO T cells relative to WT, DGKζ − / −, or Cbl - b − / − T cells at early time points (Fig. 3B, upper panels), we did not observe enhanced
granzyme B production
in DKO relative to DGKζ − / − or Cbl - b − / − T cells at later time points (Fig. 3B, lower panels), at higher or lower concentrations of anti-CD3 Ab, or with addition of anti-CD28 Ab (Supplemental Fig. 2B).
In particular, they investigate how killer immune cells use pore forming protein perforin, antimicrobial peptide granulysin, and immune protease granzyme B in synergy to destroy pathogens in host cell
In particular, they investigate how killer immune cells use pore forming protein perforin, antimicrobial peptide granulysin, and immune protease
granzyme B
in synergy to destroy pathogens in host cell
in synergy to destroy pathogens
in host cell
in host cells.
First, after culturing human peripheral blood mononuclear cells (hu - PBMCs) with the IL - 15 superagonist, flow cytometry revealed increases
in granzyme B and perforin expression
in the CD3 -, CD16 +, CD56 + NK cells.